Clinical Trial of Pregabalin and COX2 in Spinal Stenosis
Primary Purpose
Spinal Stenosis Lumbar
Status
Unknown status
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Pregabalin 75mg
Celebrex 200Mg Capsule
Sponsored by
About this trial
This is an interventional treatment trial for Spinal Stenosis Lumbar focused on measuring Pregabalin, Selective COX-2 inhibitor
Eligibility Criteria
Inclusion Criteria:
- Spinal stenosis
Exclusion Criteria:
- Koval grade >=3
- Other musculoskeletal disorders which cause pain on other joint
- Bleeding risk or ulcer history
- Severe cardiovascular, pulmonary, renal, brain, liver dysfunction
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Pregabalin and COX-2 inhibitor
COX-2 inhibitor
Arm Description
Pregabalin 75mg BID + Celecoxib 200mg qd
Celecoxib 200mg qd
Outcomes
Primary Outcome Measures
Visual analog scale
Pain score for low back and lower leg
Secondary Outcome Measures
Pain sensitivity questionnaire (PSQ)
Level of pain sensitivity
Oswestry disability index (ODI)
The self-completed questionnaire contains ten topics concerning intensity of pain, lifting, ability to care for oneself, ability to walk, ability to sit, sexual function, ability to stand, social life, sleep quality, and ability to travel
Full Information
NCT ID
NCT03584074
First Posted
June 29, 2018
Last Updated
June 29, 2018
Sponsor
Seoul National University Bundang Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03584074
Brief Title
Clinical Trial of Pregabalin and COX2 in Spinal Stenosis
Official Title
Comparative Study for Decrease of Pain Intensity and Pain Sensitivity Between Pregabalin + COX-2 Inhibitor and COX-2 Inhibitor in Patients With Lumbar Spinal Stenosis: Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
June 2018
Overall Recruitment Status
Unknown status
Study Start Date
July 1, 2018 (Anticipated)
Primary Completion Date
May 30, 2019 (Anticipated)
Study Completion Date
December 31, 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Seoul National University Bundang Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Aim of this prospective, single-blind, randomized study was to compare the efficacy of the combination of celecoxib and pregabalin and celecoxib only monotherapy for treatment of chronic low-back pain.
Detailed Description
The efficacy and safety of the association of celecoxib [a selective cyclooxygenase-2 (COX-2) inhibitor] and pregabalin (commonly used to control neuropathic pain), compared with monotherapy of each, were evaluated for the treatment of chronic low-back pain, a condition known to be due to neuropathic as well as nociceptive pain mechanisms.
We will compare the efficacy of the combination of a selective COX-2 inhibitor (celecoxib) and an antineuropathic drug, pregabalin, versus celecoxib only monotherapy, in the treatment of spinal stenosis.
Each treatment lasted 8 weeks
Primary outcome is mean pain reduction following different treatments regimes. Secondary outcomes are the changes of pain sensitivity, Oswestry disability index, adverse effects due to the treatments under study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spinal Stenosis Lumbar
Keywords
Pregabalin, Selective COX-2 inhibitor
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Pregabalin and COX-2 inhibitor
Arm Type
Experimental
Arm Description
Pregabalin 75mg BID + Celecoxib 200mg qd
Arm Title
COX-2 inhibitor
Arm Type
Active Comparator
Arm Description
Celecoxib 200mg qd
Intervention Type
Drug
Intervention Name(s)
Pregabalin 75mg
Intervention Description
Orally taken twice daily for 8 weeks
Intervention Type
Drug
Intervention Name(s)
Celebrex 200Mg Capsule
Intervention Description
Orally taken once daily for 8 weeks
Primary Outcome Measure Information:
Title
Visual analog scale
Description
Pain score for low back and lower leg
Time Frame
At 8 weeks
Secondary Outcome Measure Information:
Title
Pain sensitivity questionnaire (PSQ)
Description
Level of pain sensitivity
Time Frame
At 8 weeks
Title
Oswestry disability index (ODI)
Description
The self-completed questionnaire contains ten topics concerning intensity of pain, lifting, ability to care for oneself, ability to walk, ability to sit, sexual function, ability to stand, social life, sleep quality, and ability to travel
Time Frame
At 8 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Spinal stenosis
Exclusion Criteria:
Koval grade >=3
Other musculoskeletal disorders which cause pain on other joint
Bleeding risk or ulcer history
Severe cardiovascular, pulmonary, renal, brain, liver dysfunction
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ho-Joong Kim, M.D., Ph.D
Phone
+82317872300
Email
oshjkim@gmail.com
12. IPD Sharing Statement
Learn more about this trial
Clinical Trial of Pregabalin and COX2 in Spinal Stenosis
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